Sharp Drugs, Inc.
FDA inspection history in West Hampton Beach, New York, 2018
- 1
- Form 483
Every document, by year
- Form 483
2018: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2018One Form 483, at West Hampton Beach, New York.
Cited most
Across all Sharp Drugs observations on file
- 21 CFR 211.113Control of microbiological contamination3
- 21 CFR 211.42Design and construction features2
- 21 CFR 211.28Personnel responsibilities1
The complete Sharp Drugs file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
West Hampton Beach, New York
One Form 483 · 2018 · 6 observations
Latest: Form 483, Aug 1, 2018 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2018-08-01 | 483 Form 483 | West Hampton Beach, New York | 6 | $99 |
Investigators on these documents
FEI number 3014454961 · most recent document Aug 1, 2018
About Sharp Drugs, Inc.
How many FDA Form 483s has Sharp Drugs, Inc. received?
FDA Intel has 1 Form 483 on file for Sharp Drugs, Inc.; the most recent is dated Aug 1, 2018.
When was Sharp Drugs, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Sharp Drugs, Inc. is a Form 483 dated Aug 1, 2018, for the site in West Hampton Beach, New York.
What did FDA cite at Sharp Drugs, Inc.?
The regulations cited most in the observations on file for Sharp Drugs, Inc. are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.42 (Design and construction features), 2 times; 21 CFR 211.28 (Personnel responsibilities), 1 time.